Scanning transmission helium ion microscopy on carbon nanomembranes

• Daniel Emmrich,
• Annalena Wolff,
• Nikolaus Meyerbröker,
• Jörg K. N. Lindner,
• André Beyer and
• Armin Gölzhäuser

Beilstein J. Nanotechnol. 2021, 12, 222–231, doi:10.3762/bjnano.12.18

• photoelectron emission angle of 13° with respect to the surface normal. Energy-filtered transmission electron microscopy was conducted at energies of 60 and 80 keV on a Cs-corrected JEOL JEM-ARM200F equipped with a cold field emission gun. A GATAN GIF-Quantum ER image filter and a 2k × 2k CCD camera (GATAN

ZnO and MXenes as electrode materials for supercapacitor devices

• Ameen Uddin Ammar,
• Ipek Deniz Yildirim,
• Feray Bakan and
• Emre Erdem

Beilstein J. Nanotechnol. 2021, 12, 49–57, doi:10.3762/bjnano.12.4

• tantalum carbide MXene sheets was carried out using X-ray diffraction measurements (XRD), field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), and Raman spectroscopy. The results of XRD, FE-SEM, and Raman showed that tantalum carbide MXenes are layered solid

Bio-imaging with the helium-ion microscope: A review

• Matthias Schmidt,
• James M. Byrne and
• Ilari J. Maasilta

Beilstein J. Nanotechnol. 2021, 12, 1–23, doi:10.3762/bjnano.12.1

• resembles a field-emission scanning electron microscope (FE-SEM), but the use of helium ions rather than electrons provides several advantages, including higher surface sensitivity, larger depth of field, and a straightforward charge-compensating electron flood gun, which enables imaging of non-conductive

• opportunity for further developments. On the one hand, it is as flexible and straightforward to use as a scanning electron microscope (SEM) but with a five times larger depth of field [1] and a lateral resolution of about 0.5 nm [4] (demonstrated record: 0.24 nm [5]), which is between high-end field-emission

• milling and imaging. Plant imaging was done on the model species Arabidopsis thaliana. The HIM images of the uncoated cuticle samples showed fine textures and minute ridges not discernible in the low-voltage field-emission SEM images of the same samples. Arabidopsis samples were also HIM-imaged by Curtin

Oxidation of Au/Ag films by oxygen plasma: phase separation and generation of nanoporosity

• Abdel-Aziz El Mel,
• Said A. Mansour,
• Mujaheed Pasha,
• Atef Zekri,
• Janarthanan Ponraj,
• Akshath Shetty and
• Yousef Haik

Beilstein J. Nanotechnol. 2020, 11, 1608–1614, doi:10.3762/bjnano.11.143

• current of the X-ray generator were set to 45 kV and 40 mA, respectively. The signal was collected between 20° and 90° with a step size of 0.02° and at a speed of 1 deg/min. STEM and STEM-EDS were performed on a TALOS (FEI, Hillsboro, Oregon, USA) field emission gun transmission electron microscope

Walking energy harvesting and self-powered tracking system based on triboelectric nanogenerators

• Mingliang Yao,
• Guangzhong Xie,
• Qichen Gong and
• Yuanjie Su

Beilstein J. Nanotechnol. 2020, 11, 1590–1595, doi:10.3762/bjnano.11.141

• the electrode as an output terminal. Characterization and electrical measurement of the u-TENG Field-emission scanning electron microscopy (FESEM, Hitachi SU-8020) was used to characterize the surface morphology of the modified PTFE film. A Stanford Research Systems equipment was used to measure the

Structure and electrochemical performance of electrospun-ordered porous carbon/graphene composite nanofibers

• Yi Wang,
• Yanhua Song,
• Chengwei Ye and
• Lan Xu

Beilstein J. Nanotechnol. 2020, 11, 1280–1290, doi:10.3762/bjnano.11.112

• electron microscopy (SEM) under a field-emission scanning electron microscope (FE-SEM) (Hitachi, S4800, Japan). The structural characteristics of the CNFs were observed via transmission electron microscopy (TEM) (FEI, Tecnai G20, Japan). The diameter values of the CNFs were measured using ImageJ software

Ultrasensitive detection of cadmium ions using a microcantilever-based piezoresistive sensor for groundwater

• Dinesh Rotake,
• Anand Darji and
• Nitin Kale

Beilstein J. Nanotechnol. 2020, 11, 1242–1253, doi:10.3762/bjnano.11.108

• ) LOD, which is well below the WHO limit for cadmium ions. The paper describes the methodology, the formation of SAMs and their characterization using field-emission scanning electron microscopy (FESEM), the use of the portable experimental platform with the MEMS-based piezoresistive device to selective

Magnetic-field-assisted synthesis of anisotropic iron oxide particles: Effect of pH

• Andrey V. Shibaev,
• Petr V. Shvets,
• Darya E. Kessel,
• Roman A. Kamyshinsky,
• Anton S. Orekhov,
• Sergey S. Abramchuk,
• Alexei R. Khokhlov and
• Olga E. Philippova

Beilstein J. Nanotechnol. 2020, 11, 1230–1241, doi:10.3762/bjnano.11.107

• scanning TEM (STEM). The specimens were examined under a TITAN 80-300 microscope (FEI, USA) equipped with a Schottky field emission gun, a spherical aberration corrector (Cs probe corrector), a direct detection camera (Falcon II, FEI, USA), and an EDX spectroscopy system (EDAX, USA). The TEM was operated

3D superconducting hollow nanowires with tailored diameters grown by focused He⁺ beam direct writing

• Rosa Córdoba,
• Alfonso Ibarra,
• Dominique Mailly,
• Isabel Guillamón,
• Hermann Suderow and
• José María De Teresa

Beilstein J. Nanotechnol. 2020, 11, 1198–1206, doi:10.3762/bjnano.11.104

• operated at 300 kV and equipped with a high-brightness X-FEG and a CETCOR Cs corrector for the condenser system to provide sub-angstrom probe size. STEM high-angle annular dark-field (HAADF) tomography was performed using a Thermo Fisher Tecnai field-emission gun operated at 300 kV. The angular range for

Highly sensitive detection of estradiol by a SERS sensor based on TiO₂ covered with gold nanoparticles

• Andrea Brognara,
• Ili F. Mohamad Ali Nasri,
• Beatrice R. Bricchi,
• Andrea Li Bassi,
• Caroline Gauchotte-Lindsay,
• Matteo Ghidelli and
• Nathalie Lidgi-Guigui

Beilstein J. Nanotechnol. 2020, 11, 1026–1035, doi:10.3762/bjnano.11.87

• . The thermal treatment was carried out to induce both crystallization of the as-deposited amorphous TiO2 into the anatase phase (as discussed in [28][29]) and the formation of AuNPs exploiting dewetting of the Au films. A field-emission scanning electron microscope (FEG-SEM, Zeiss Supra 40) was used to

Microwave-induced electric discharges on metal particles for the synthesis of inorganic nanomaterials under solvent-free conditions

• Vijay Tripathi,
• Harit Kumar,
• Anubhav Agarwal and
• Leela S. Panchakarla

Beilstein J. Nanotechnol. 2020, 11, 1019–1025, doi:10.3762/bjnano.11.86

• supernatant solution is collected for further characterization. Characterization of products The reaction products are characterized by X-ray diffraction (PANanalytical X’pert PRO), field-emission scanning electron microscopy (JEOL JSM 7600F, combined with energy-dispersive spectroscopy (EDS)), transmission

Wet-spinning of magneto-responsive helical chitosan microfibers

• Dorothea Brüggemann,
• Johanna Michel,
• Naiana Suter,
• Matheus Grande de Aguiar and
• Michael Maas

Beilstein J. Nanotechnol. 2020, 11, 991–999, doi:10.3762/bjnano.11.83

• scanning electron microscope (SEM) using a Zeiss Supra 40 field-emission device (Carl Zeiss, Oberkochen, Germany) at an acceleration voltage of 3 kV. Prior to SEM analysis, dried fibers were sputter-coated with a 7 nm gold layer using a Bal-Tec SCD 005 sputter system (Leica Microsystems, Wetzlar, Germany

Electrochemical nanostructuring of (111) oriented GaAs crystals: from porous structures to nanowires

• Elena I. Monaico,
• Eduard V. Monaico,
• Veaceslav V. Ursaki,
• Shashank Honnali,
• Vitalie Postolache,
• Karin Leistner,
• Kornelius Nielsch and
• Ion M. Tiginyanu

Beilstein J. Nanotechnol. 2020, 11, 966–975, doi:10.3762/bjnano.11.81

• these nanowires were tested for field emission, but not for photodetector applications. The nanowires were produced using electrochemical etching under optimized conditions in a mixed H3PO4/HCl electrolyte followed by chemical etching for reducing the diameter down to 150 nm. The authors of the work did

A set of empirical equations describing the observed colours of metal–anodic aluminium oxide–Al nanostructures

• Cristina V. Manzano,
• Jakob J. Schwiedrzik,
• Gerhard Bürki,
• Laszlo Pethö,
• Johann Michler and
• Laetitia Philippe

Beilstein J. Nanotechnol. 2020, 11, 798–806, doi:10.3762/bjnano.11.64

• (yielding to the same porosity), changing only the second anodization time (from 120 to 600 s) to obtain different film thicknesses (from 209 ± 12 nm to 380 ± 15 nm). Focused ion beam (FIB) milling and field-emission scanning electron microscopy (FESEM) imaging were used to accurately determine the

• . After that, the Cr layer was deposited. Characterization of AAO films Morphological characterisation was performed using a field-emission scanning electron microscope (FESEM, Hitachi S-4800) with a 1.5 kV accelerating voltage. The thickness was obtained from sample cross sections fabricated using a

Effect of Ag loading position on the photocatalytic performance of TiO₂ nanocolumn arrays

• Jinghan Xu,
• Yanqi Liu and
• Yan Zhao

Beilstein J. Nanotechnol. 2020, 11, 717–728, doi:10.3762/bjnano.11.59

• structures were observed using a field emission scanning electron microscope (FE-SEM, FEI, Tecnai G2 F30). The elemental composition and valence distribution of the film were measured by X-ray photoelectron spectroscopy (XPS, Thermo Fisher Scientific, ESCALAB 250Xi). The photoluminescence (PL) intensity of

Structural optical and electrical properties of a transparent conductive ITO/Al–Ag/ITO multilayer contact

• Aliyu Kabiru Isiyaku,
• Ahmad Hadi Ali and
• Nafarizal Nayan

Beilstein J. Nanotechnol. 2020, 11, 695–702, doi:10.3762/bjnano.11.57

• IAAI and ITO films was further analyzed by field-emission scanning electron microscopy (FESEM, 5.0 kV, 100000× magnification). Figure 4 shows FESEM images of the as-deposited and annealed IAAI and ITO films. The as-deposited IAAI and ITO films show a smooth and continuous surface with small grains and

• carried out using the Nanoscope Analysis software. All films were scanned over an area of 1 μm × 1 μm. Field-emission scanning electron microscopic analyses The surface morphology of the prepared thin films was further studied using field-emission scanning electron microscopy (FESEM). A FESEM JEOL JSM

Exfoliation in a low boiling point solvent and electrochemical applications of MoO₃

• Matangi Sricharan,
• Bikesh Gupta,
• Sreejesh Moolayadukkam and
• H. S. S. Ramakrishna Matte

Beilstein J. Nanotechnol. 2020, 11, 662–670, doi:10.3762/bjnano.11.52

• preheated oven. The remaining MoO3 powder in the beaker was weighed to determine the concentration. The morphology of MoO3 flakes was characterized using field-emission scanning electron microscopy (FESEM; Tescan Mira3), transmission electron microscopy (TEM; FEI Talos, 200 kV) and atomic force microsopy

Silver-decorated gel-shell nanobeads: physicochemical characterization and evaluation of antibacterial properties

• Marta Bartel,
• Katarzyna Markowska,
• Marcin Strawski,
• Krystyna Wolska and
• Maciej Mazur

Beilstein J. Nanotechnol. 2020, 11, 620–630, doi:10.3762/bjnano.11.49

• ) analysis were performed with a Zeiss Merlin field-emission SEM instrument. Transmission electron microscopy images were collected with a Zeiss Libra 120 EFTEM. Confocal laser scanning microscopy (CLSM) imaging of bacterial biofilms was performed with a Nikon AIR MP microscope equipped with a 60×, NA 1.4

Synthesis and enhanced photocatalytic performance of 0D/2D CuO/tourmaline composite photocatalysts

• Changqiang Yu,
• Min Wen,
• Zhen Tong,
• Shuhua Li,
• Yanhong Yin,
• Xianbin Liu,
• Yesheng Li,
• Tongxiang Liang,
• Ziping Wu and
• Dionysios D. Dionysiou

Beilstein J. Nanotechnol. 2020, 11, 407–416, doi:10.3762/bjnano.11.31

• using step scan mode performed with a DX-2700 diffractometer (Dandong Haoyuan Instrument Co. Ltd., China) with Ni-filtered Cu Kα radiation (λ = 0.1.541 Å), 10–80° 2θ scan. X-ray photoelectron spectra (XPS) were recorded using a K-ALPHA instrument (ThermoFisher Scientific, USA). A MIRA3 field emission

Poly(1-vinylimidazole) polyplexes as novel therapeutic gene carriers for lung cancer therapy

• Gayathri Kandasamy,
• Elena N. Danilovtseva,
• Vadim V. Annenkov and
• Uma Maheswari Krishnan

Beilstein J. Nanotechnol. 2020, 11, 354–369, doi:10.3762/bjnano.11.26

• RNAse-free water and dried overnight. The samples were stained with 1% phosphotungstic acid solution (Merck, Germany) and imaged using high-resolution field-emission transmission electron microscopy (JEM2100F, JEOL, Japan). Differential scanning calorimetry: The melting point of the blank PVI

• . Characterization of the polyplex Electron microscopy: A small drop of the polyplex sample was placed on a conducting carbon tape and air-dried. The sample was then sputter-coated with a thin film of gold. The sample was placed in the sample chamber and imaged at an accelerating voltage of 3 kV using a cold field

• -emission scanning electron microscope (JSM6701F, JEOL, Japan). For transmission electron microscopy, 1 mL of the polyplex was deposited on 400 mesh copper grids (Canemco-Marivac, Canada) and air-dried for 10 min. The excess sample was removed by blotting using a filter paper. The grids were washed using

Simple synthesis of nanosheets of rGO and nitrogenated rGO

• Pallellappa Chithaiah,
• Madhan Mohan Raju,
• Giridhar U. Kulkarni and
• C. N. R. Rao

Beilstein J. Nanotechnol. 2020, 11, 68–75, doi:10.3762/bjnano.11.7

• Mira3 field-emission scanning electron microscope (FESEM) equipped with an energy-dispersive X-ray spectroscopy (EDS). The TEM, HRTEM images and SAED patterns were obtained on a TALOS F200S G2, 200 kV FEG, and a CMOS camera (4k × 4k). The TEM samples were prepared by suspending the samples in ethanol

Synthesis of amorphous and graphitized porous nitrogen-doped carbon spheres as oxygen reduction reaction catalysts

• Maximilian Wassner,
• Markus Eckardt,
• Andreas Reyer,
• Thomas Diemant,
• Michael S. Elsaesser,
• R. Jürgen Behm and
• Nicola Hüsing

Beilstein J. Nanotechnol. 2020, 11, 1–15, doi:10.3762/bjnano.11.1

• Scanning electron microscopy (SEM) images were recorded with a field-emission scanning electron microscope (FE-SEM, Zeiss Ultra Plus) at 10 to 12 keV beam energy. For imaging, the samples were deposited on a conducting carbon film. Energy-dispersive X-ray spectroscopy (EDX) measurements were performed on

Synthesis and acetone sensing properties of ZnFe₂O₄/rGO gas sensors

• Kaidi Wu,
• Yifan Luo,
• Ying Li and
• Chao Zhang

Beilstein J. Nanotechnol. 2019, 10, 2516–2526, doi:10.3762/bjnano.10.242

• ZnFe2O4. In addition, the results of field-emission scanning electron microscopy and (high-resolution) transmission electron microscopy indicated that the synthesized samples had the structure of hollow spheres distributed uniformly onto rGO nanosheets. The diameters of the spheres were determined as

• diffraction (XRD, Bruker D8 Advance) using Cu Kα radiation at room temperature. The 2θ range was 10−80°, and the scanning rate was 5°·min−1. The microscopic morphology and the size of all samples were observed using a field-emission scanning electron microscope equipped with an energy-dispersive spectrometer

• (FESEM, Hitachi S4800). The nanostructure of the products was examined by transmission electron microscopy (TEM, JEM-2100). High-resolution TEM (HRTEM) and energy-dispersive X-ray (EDX) elemental mappings were recorded using a field-emission transmission electron microscope (Tecnai G2 F30 S-TWIN, FEI

Polyvinylpyrrolidone as additive for perovskite solar cells with water and isopropanol as solvents

• Chen Du,
• Shuo Wang,
• Xu Miao,
• Wenhai Sun,
• Yu Zhu,
• Chengyan Wang and
• Ruixin Ma

Beilstein J. Nanotechnol. 2019, 10, 2374–2382, doi:10.3762/bjnano.10.228

• chlorobenzene) at 4500 rpm for 20 s. The above preparation process was carried out under ambient conditions. Finally, the devices were completed by using thermal evaporation and deposited on an Au electrode. Characterization Field-emission scanning electron microscopy (FESEM) images were obtained with a ZEISS

Design and facile synthesis of defect-rich C-MoS₂/rGO nanosheets for enhanced lithium–sulfur battery performance

• Chengxiang Tian,
• Juwei Wu,
• Zheng Ma,
• Bo Li,
• Pengcheng Li,
• Xiaotao Zu and
• Xia Xiang

Beilstein J. Nanotechnol. 2019, 10, 2251–2260, doi:10.3762/bjnano.10.217

• -4, C-MoS2/rGO-6, C-MoS2/rGO-8) with a 3:1 mass ratio was calcined at 155 °C for 12 h in a sealed vessel. Materials characterization The structure and morphology were investigated by field-emission scanning electron microscopy (FE-SEM, INSPECT F50) and transmission electron microscopy (TEM, ZEISS